CN116825310A - Clinical trial medicine management method and system for intelligent medicine cabinet - Google Patents
Clinical trial medicine management method and system for intelligent medicine cabinet Download PDFInfo
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- 239000003814 drug Substances 0.000 title claims abstract description 545
- 238000007726 management method Methods 0.000 title claims abstract description 33
- 229940079593 drug Drugs 0.000 claims abstract description 206
- 238000012360 testing method Methods 0.000 claims abstract description 97
- 230000008859 change Effects 0.000 claims abstract description 54
- 238000000034 method Methods 0.000 claims description 35
- 238000011084 recovery Methods 0.000 claims description 9
- 238000003860 storage Methods 0.000 description 7
- 238000004590 computer program Methods 0.000 description 4
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- 230000001360 synchronised effect Effects 0.000 description 3
- 239000002775 capsule Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 229960003088 loratadine Drugs 0.000 description 2
- JCCNYMKQOSZNPW-UHFFFAOYSA-N loratadine Chemical compound C1CN(C(=O)OCC)CCC1=C1C2=NC=CC=C2CCC2=CC(Cl)=CC=C21 JCCNYMKQOSZNPW-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
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- 230000004048 modification Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
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- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
- G16H40/20—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06K—GRAPHICAL DATA READING; PRESENTATION OF DATA; RECORD CARRIERS; HANDLING RECORD CARRIERS
- G06K19/00—Record carriers for use with machines and with at least a part designed to carry digital markings
- G06K19/06—Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the kind of the digital marking, e.g. shape, nature, code
- G06K19/067—Record carriers with conductive marks, printed circuits or semiconductor circuit elements, e.g. credit or identity cards also with resonating or responding marks without active components
- G06K19/07—Record carriers with conductive marks, printed circuits or semiconductor circuit elements, e.g. credit or identity cards also with resonating or responding marks without active components with integrated circuit chips
- G06K19/0723—Record carriers with conductive marks, printed circuits or semiconductor circuit elements, e.g. credit or identity cards also with resonating or responding marks without active components with integrated circuit chips the record carrier comprising an arrangement for non-contact communication, e.g. wireless communication circuits on transponder cards, non-contact smart cards or RFIDs
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06K—GRAPHICAL DATA READING; PRESENTATION OF DATA; RECORD CARRIERS; HANDLING RECORD CARRIERS
- G06K7/00—Methods or arrangements for sensing record carriers, e.g. for reading patterns
- G06K7/10—Methods or arrangements for sensing record carriers, e.g. for reading patterns by electromagnetic radiation, e.g. optical sensing; by corpuscular radiation
- G06K7/10009—Methods or arrangements for sensing record carriers, e.g. for reading patterns by electromagnetic radiation, e.g. optical sensing; by corpuscular radiation sensing by radiation using wavelengths larger than 0.1 mm, e.g. radio-waves or microwaves
- G06K7/10297—Methods or arrangements for sensing record carriers, e.g. for reading patterns by electromagnetic radiation, e.g. optical sensing; by corpuscular radiation sensing by radiation using wavelengths larger than 0.1 mm, e.g. radio-waves or microwaves arrangements for handling protocols designed for non-contact record carriers such as RFIDs NFCs, e.g. ISO/IEC 14443 and 18092
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Abstract
The embodiment of the application discloses a clinical trial medicine management method for an intelligent medicine cabinet, which comprises the following steps: receiving a cabinet entering list of tested medicines, wherein the cabinet entering list comprises first tested medicine information, and the tested medicines are provided with unique electronic tags; when detecting that the tested medicine is put on the bearing table, acquiring first weight change information corresponding to the pressure sensor; when the cabinet door is detected to be closed, the RFID reader-writer scans the electronic tag of the tested medicine, acquires tag information of the tested medicine and matches the tag information with the first tested medicine information; if the matching is successful, acquiring the position information of the tested medicine according to the label information and the first weight change information of the tested medicine; receiving a dispensing list of the test drug, the dispensing list including subject information and second test drug information; when the cabinet door is detected to be opened, the bearing table corresponding to the tested medicine is prompted according to the second tested medicine information and the position information of the tested medicine.
Description
Technical Field
The application relates to the technical field of medical appliances, in particular to a clinical trial medicine management method and system for an intelligent medicine cabinet.
Background
GCP (Good Clinical Practice) is the quality management standard of the current clinical test of the medicine in China, and is the standard and standardized management regulation of the clinical test by the national medicine supervision and management department; the purpose of GCP is to ensure the normative and reliable clinical test process, scientific and credible results and the rights and life safety of the subjects; in short, GCP is a guideline for conducting clinical trials that is formulated to ensure the quality of clinical trial data, protect the safety and rights of subjects.
In the prior art, due to the management, the validity period and the specificity of a subject of clinical test medicines, the traditional medicine management mode is used for managing clinical test medicines, so that the efficiency is low, the distribution errors are easy to occur, and the distribution flow of the clinical test medicines is more complex; therefore, the application provides a clinical trial medicine management method of an intelligent medicine cabinet related to GCP, which realizes the overall standard management of clinical trial medicines.
Disclosure of Invention
Based on this, it is necessary to address the above-mentioned problems, and a clinical trial drug management method for an intelligent drug cabinet is proposed.
The utility model provides a clinical trial medicine management method for intelligent medicine cabinet, intelligent medicine cabinet includes cabinet body, RFID read write line, a plurality of plummer and a plurality of pressure sensor, the RFID read write line sets up in the cabinet body, a plurality of pressure sensor respectively one by one with a plurality of plummer corresponds, its characterized in that, the method includes:
receiving a cabinet entering list of tested medicines, wherein the cabinet entering list comprises first tested medicine information, and the tested medicines are provided with unique electronic tags;
when the tested medicine is detected to be placed on the bearing table, acquiring first weight change information corresponding to the pressure sensor;
when the cabinet door is detected to be closed, the RFID reader-writer scans the electronic tag of the tested medicine, acquires tag information of the tested medicine and matches the tag information with the first tested medicine information;
if the matching is successful, acquiring the position information of the tested medicine according to the label information of the tested medicine and the first weight change information;
receiving a release list of the tested drugs, wherein the release list comprises subject information and second tested drug information;
when the cabinet door is detected to be opened, the bearing table corresponding to the tested medicine is prompted according to the second tested medicine information and the position information of the tested medicine.
In the above scheme, the method further comprises:
receiving a recovery list of the to-be-recovered test drug, wherein the recovery list comprises third test drug information;
when the to-be-recovered tested medicine is detected to be placed on the bearing table, second weight change information corresponding to the pressure sensor is obtained;
when the cabinet door is detected to be closed, the RFID reader-writer scans the electronic tag of the to-be-recovered tested medicine, acquires tag information of the to-be-recovered tested medicine and matches the tag information with the third tested medicine information, and if matching is successful, acquires the position information of the to-be-recovered tested medicine according to the tag information of the to-be-recovered tested medicine and the second weight change information.
In the above scheme, the method further comprises:
generating a return list of the tested medicines according to the third tested medicine information and/or the expired medicine information;
when the cabinet door is detected to be opened, prompting a bearing table corresponding to the tested medicine to be recovered according to the third tested medicine information and the position information of the tested medicine to be recovered; and/or prompting a bearing table corresponding to the expired tested medicine according to the expired medicine information and the position information of the tested medicine.
In the above-mentioned scheme, the cabinet body includes upper cabinet and lower floor's cabinet, before step when detecting the test medicine is put into on the plummer, obtain corresponding pressure sensor's first weight change information, the method still includes:
and according to the first tested medicine information and the position information of the tested medicine in the current cabinet body, acquiring the position information of the same kind of medicine as the tested medicine, distributing the tested medicine to the corresponding bearing table, and correspondingly opening the cabinet door of the upper cabinet or the lower cabinet layer.
In the above-mentioned scheme, according to the first test medicine information and the current position information of the test medicine in the cabinet body, obtain the position information that is the same kind of medicine with the test medicine, distribute the test medicine to the plummer that corresponds to, and correspond the step of opening the cabinet door of upper cabinet or lower cabinet layer still includes:
if the upper cabinet and the lower cabinet are provided with the tested medicine corresponding to the first tested medicine information, acquiring the current weight information of the bearing table, which is the same medicine as the tested medicine, in the cabinet body, distributing the tested medicine to the bearing table with the minimum weight, and opening the corresponding cabinet door of the upper cabinet or the lower cabinet.
In the above scheme, before the step of obtaining the first weight change information corresponding to the pressure sensor when the tested drug is detected to be placed on the bearing table, the method further includes:
if the types of the tested medicines corresponding to the first tested medicine information are multiple, the current weight information of each layer of the loading table in the cabinet body is obtained, the multiple tested medicines are distributed to the loading table with the minimum weight, and the corresponding cabinet door of the upper cabinet or the lower cabinet is opened.
In the above aspect, a dispensing list of the test drug is received, the dispensing list including subject information and second test drug information, and then the method further includes:
determining a matching list of the subject and the test drug according to the subject information and the second test drug information:
acquiring the corresponding relation between the subject and the tested medicine according to the matching list of the subject and the tested medicine;
determining whether the dispensed test drug is correct according to the corresponding relation between the subject and the test drug; wherein, the corresponding relation is a one-to-one or one-to-many matching relation between the subject and the tested medicine.
In the above scheme, the method further comprises the steps of:
when the inventory of the tested medicines matched with the subjects is at least two, acquiring one of the tested medicines with the shortest near-term;
and prompting the corresponding bearing table of the tested drug with the shortest near-term according to the second tested drug information and the position information of the tested drug.
In the above solution, before the step of obtaining the second weight change information corresponding to the pressure sensor when the test drug to be recovered is detected to be placed on the carrying platform, the method further includes:
and acquiring the position information of the tested medicine to be recovered according to the position information of the tested medicine corresponding to the second tested medicine information, and prompting the bearing table corresponding to the tested medicine to be recovered according to the third tested medicine information and the position information of the tested medicine to be recovered.
The application also provides a clinical trial medicine management system for the intelligent medicine cabinet, which comprises: the device comprises a list acquisition unit, a weight change information acquisition unit and a tested drug grade position determination unit;
the list acquisition unit is used for receiving a cabinet entering list of the tested medicines and a dispensing list of the tested medicines, wherein the cabinet entering list comprises first tested medicine information, and the tested medicines are provided with unique electronic tags; the release list comprises subject information and second test drug information;
the weight change information acquisition unit is used for acquiring weight change information of the corresponding pressure sensor when the tested medicine is detected to be placed on the bearing table;
the test medicine grade position determining unit is used for scanning the electronic tag of the test medicine when the cabinet door is detected to be closed, acquiring tag information of the test medicine and matching the tag information with the first test medicine information, acquiring position information of the test medicine according to the tag information of the test medicine and the first weight change information if matching is successful, and prompting a bearing table corresponding to the test medicine according to the second test medicine information and the position information of the test medicine when the cabinet door is detected to be opened.
The embodiment of the application has the following beneficial effects: the method comprises the steps of receiving a cabinet entering list of tested medicines, wherein the cabinet entering list comprises first tested medicine information, and the tested medicines are provided with unique electronic tags; when the tested medicine is detected to be placed on the bearing table, acquiring first weight change information corresponding to the pressure sensor; when the cabinet door is detected to be closed, the RFID reader-writer scans the electronic tag of the tested medicine, acquires tag information of the tested medicine and matches the tag information with the first tested medicine information; if the matching is successful, acquiring the position information of the tested medicine according to the label information of the tested medicine and the first weight change information; receiving a release list of the tested drugs, wherein the release list comprises subject information and second tested drug information; when the cabinet door is detected to be opened, the bearing table corresponding to the tested medicine is prompted according to the second tested medicine information and the position information of the tested medicine.
Drawings
In order to more clearly illustrate the embodiments of the application or the technical solutions in the prior art, the drawings that are required in the embodiments or the description of the prior art will be briefly described, it being obvious that the drawings in the following description are only some embodiments of the application, and that other drawings may be obtained according to these drawings without inventive effort for a person skilled in the art.
Wherein:
FIG. 1 is a schematic structural diagram of an intelligent medicine cabinet;
FIG. 2 is a schematic view of the structure of the carrying platform in FIG. 1;
FIG. 3 is a flow chart of a method of clinical trial drug management for an intelligent drug cabinet in one embodiment;
FIG. 4 is a flow chart of determining whether the test drug in the cabinet is correct according to the correspondence between the subject and the test drug in one embodiment;
FIG. 5 is a flow chart of determining whether a received test drug is correct according to a matching relationship between test drug information and third test drug information in an embodiment;
FIG. 6 is a flow chart of acquiring a test drug return list and location information of a test drug to be recovered in one embodiment;
FIG. 7 is a flow chart of a return step in a drug management method of the intelligent medicine cabinet in one embodiment.
Detailed Description
The following description of the embodiments of the present application will be made clearly and completely with reference to the accompanying drawings, in which it is apparent that the embodiments described are only some embodiments of the present application, but not all embodiments. All other embodiments, which can be made by those skilled in the art based on the embodiments of the application without making any inventive effort, are intended to be within the scope of the application.
In the following description, numerous specific details are set forth in order to provide a more thorough understanding of the present application. It will be apparent, however, to one skilled in the art that the application may be practiced without one or more of these details. In other instances, well-known features have not been described in detail in order to avoid obscuring the application. It should be understood that the present application may be embodied in various forms and should not be construed as limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the application to those skilled in the art.
The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the application. As used herein, the singular forms "a," "an," and "the" are intended to include the plural forms as well, unless the context clearly indicates otherwise, and it is to be understood that the terms "comprises" and/or "comprising" when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof. As used herein, the term "and/or" includes any and all combinations of the associated listed items.
In order to thoroughly understand the present application, a detailed structure will be presented in the following description to explain the technical scheme presented in the present application, and the clinical test medicine management method for an intelligent medicine cabinet disclosed in the present application may be used for an intelligent medicine cabinet, as shown in fig. 1, where the medicine cabinet includes a cabinet body and a cabinet door, a bearing table is provided in the cabinet body, the bearing table is connected with the inside of the cabinet body through a fixing frame, the bearing table may be provided with multiple layers, throughout the inside of the cabinet body, each layer of bearing table includes a carrier plate and a pressure sensor disposed under the carrier plate, and the pressure sensor may sense a weight change of a medicine on the bearing table to identify whether the medicine is taken or put in; wherein, the clinical test medicine is the tested medicine.
As shown in fig. 2, the front end of the loading table is provided with an LED screen, a pressure sensor is correspondingly arranged below the loading table, an RFID reader is arranged on the side wall in the cabinet, the two sides of the loading table are symmetrically arranged, when taking medicine, the medicine distributed by the system is prompted on the LED screen of the corresponding layer, when the action of taking medicine is completed, the pressure sensor senses that the medicine is taken away, and feeds back the total weight of the medicine of the loading table layer to the system, so that the number of layers corresponding to the medicine supplementing and returning is distributed according to corresponding data, the quantity of each layer is ensured to be uniform, the weight is uniform, and the interference caused to the reading of the RFID is small.
When the medicine is put, after the cabinet door is opened, the corresponding screen of the bearing table is lightened to prompt the medicine to be put into the layer, and when the medicine is put into one layer, the pressure sensor senses that the medicine is correct, and the screen on the bearing table indicates that the medicine is correct; if the pressure sensor is placed on two layers, the pressure sensor on the layer senses errors, and a screen on the bearing table is lightened and indicates the errors.
Furthermore, the medicine cabinet can prompt the required medicine on the layer, so that the medicine can be conveniently searched on the layer, when the pressure sensor senses and takes away the medicine, the screen on the bearing table of the corresponding layer is lightened, the corresponding medicine is taken away, if the wrong layer is taken, the screen on the bearing table of the corresponding layer is lightened, the error is indicated, and the error is prompted.
Preferably, the cabinet body is internally provided with a refrigerator which is used for controlling the temperature in the cabinet to be kept in a reasonable range, the specific temperature is controlled between 2 degrees and 8 degrees, the dynamic temperature is kept in the range, the cabinet body is also provided with a temperature sensor, when the temperature exceeds a numerical range, a signal can be sent out to a mobile terminal, such as a mobile phone, and the mobile phone is convenient for an instrument manager to monitor the state of the intelligent medicine cabinet.
Preferably, the cabinet body is also provided with a humidity regulator, the humidity in the control cabinet is dynamically regulated between 35% and 75%, the cabinet body is also provided with a humidity sensor, when the humidity exceeds a numerical range, a signal can be sent out to a mobile terminal, such as a mobile phone, and the mobile phone is convenient for an instrument manager to monitor the state of the intelligent medicine cabinet.
Alternative embodiments of the application are described in detail below, however, the application may have other implementations in addition to these detailed descriptions.
As shown in fig. 3, in one embodiment, a clinical trial drug management method for a smart drug cabinet is provided,
the intelligent medicine cabinet comprises a cabinet body, an RFID reader-writer, a plurality of bearing tables and a plurality of pressure sensors, wherein the RFID reader-writer is arranged in the cabinet body, the plurality of pressure sensors respectively correspond to the plurality of bearing tables one by one, and the medicine management method for the intelligent medicine cabinet comprises the following steps of S101 to S106, and is detailed as follows:
s101, receiving a cabinet entering list of tested medicines, wherein the cabinet entering list comprises first tested medicine information, and the tested medicines are provided with unique electronic tags;
in some embodiments, the tested medicines are all stuck with unique electronic tags, and the electronic tags record information of the tested medicines and comprise information of names, quantity, validity periods, commodity codes, specification models, lot numbers, departments and the like of the tested medicines.
S102, when detecting that a tested drug is placed on a bearing table, acquiring first weight change information corresponding to a pressure sensor;
specifically, when the tested medicine is placed in the A1 bearing platform, the corresponding pressure sensor under the A1 bearing platform can generate a pressure change signal, a weight change value is calculated, and the first weight change information of the corresponding pressure sensor of the A1 bearing platform is obtained by demodulating parameters such as amplitude, frequency and the like of the signal. The first weight change information may be a specific value, for example, the weight of the tested medicine, or may be a signal, for example, a fluctuation signal for detecting a change in the pressure value.
Preferably, the intelligent medicine cabinet can automatically prompt and dispense which layer the medicine should be replenished according to the existing weight of each layer.
S103, when the cabinet door is detected to be closed, the RFID reader-writer scans the electronic tag of the tested medicine, acquires tag information of the tested medicine and matches the tag information with the first tested medicine information;
the RFID reader-writer is also called reader or interrogator, is a device for reading and writing the memory information of the electronic tag, and can be in wireless communication with the electronic tag through an antenna, and can be connected with a computer network to finish the storage and management of data. In some embodiments, if the read label information of the test drug and the first test drug information may match, it is indicated that the packaged test drug is a drug in the packaged inventory.
S104, if the matching is successful, acquiring position information corresponding to the tested drug according to the label information and the first weight change information of the tested drug;
in some embodiments, the RFID reader reads the electronic tag of a certain tested drug, so that the unique identity and information of the drug can be identified, including the information of the name, validity period, commodity code, specification model, lot number, department, etc. of the tested drug, for example, the name of the drug is determined as follows: and determining the corresponding position information of the loratadine capsule in the intelligent medicine cabinet according to the first weight change information generated by the bearing table where the loratadine capsule is positioned.
In some embodiments, if the matching is unsuccessful, the intelligent drug cabinet sends out an error warning message, so that a manager can find out the error and timely replace the tested drugs in the cabinet.
S105, receiving a dispensing list of the tested medicines, wherein the dispensing list comprises subject information and second tested medicine information;
specifically, the subject information includes the name, sex, age, drug information to be tested, and the like of the subject; the second tested medicine information is medicine to be dispensed in the clinical test, and comprises the information of medicine name, quantity, production date, validity period, commodity code, specification model, batch number, department and the like of the tested medicine.
S106, when the cabinet door is detected to be opened, prompting a bearing table corresponding to the tested medicine according to the second tested medicine information and the position information of the tested medicine.
When the cabinet door is opened, the screen lamp on the bearing table corresponding to the tested medicine is lighted, the tested medicine is prompted to exist on the bearing table, and only the medicine position is required to be quickly located by searching, so that the cabinet door opening time is shortened.
In some embodiments, when the cabinet door is detected to be closed, the RFID reader scans the electronic tag of the tested medicine in the current cabinet, acquires the tag information of the tested medicine in the current cabinet and matches with the second tested medicine information; if the matching is successful, if the reduced label information corresponds to the information of the test drug to be taken out, the taken out test drug is proved to be correct.
In summary, the solution of the present application includes receiving a cabinet entry list of a tested drug, which includes first tested drug information, where the tested drug is provided with a unique electronic tag; when detecting that the tested medicine is put on the bearing table, acquiring first weight change information corresponding to the pressure sensor; when the cabinet door is detected to be closed, the RFID reader-writer scans the electronic tag of the tested medicine, acquires tag information of the tested medicine and matches the tag information with the first tested medicine information; if the matching is successful, acquiring position information corresponding to the tested medicine according to the label information and the first weight change information of the tested medicine; receiving a release list of the tested medicine, which comprises the subject information and the second tested medicine information; when the cabinet door is detected to be opened, the carrying table corresponding to the tested medicine is prompted according to the second tested medicine information and the position information of the tested medicine, the identity of the tested medicine is determined through the RFID technology, the correctness of the tested medicine is guaranteed, the tested medicine and the position are bound together by combining weighing identification of the pressure sensor, the position of the tested medicine in the medicine cabinet can be rapidly positioned, convenience is brought to a user to inquire and realize that the accuracy of medicine operation is improved in the medicine putting and taking-out process, the opening time can be shortened, and therefore the temperature return time of the tested medicine is shortened.
As shown in fig. 4, in some embodiments, the clinical trial drug management method for the intelligent drug cabinet further comprises:
s501, determining a matching list of the subject and the tested drug according to the subject information and the second tested drug information:
s502, acquiring a corresponding relation between a subject and a tested medicine according to a matching list of the subject and the tested medicine;
s503, determining whether the dispensed test drug is correct according to the corresponding relation between the subject and the test drug; wherein, the corresponding relation is a one-to-one or one-to-many matching relation between the subject and the tested medicine.
Preferably, before determining whether the dispensed test drug is correct according to the correspondence between the subject and the test drug, the method further comprises:
when the inventory of the tested medicines matched with the subjects is at least two, acquiring one of the tested medicines with the shortest near-term;
and prompting the corresponding bearing table of the tested drug with the shortest near-term according to the second tested drug information and the position information of the tested drug.
In this embodiment, if more than two tested medicines are in the medicine cabinet in the medicine dispensing process, the same kind of medicines are screened out, the information of the tested medicines is compared one by one, the tested medicines with the shortest near-term are screened out, and are preferentially dispensed, so that the risk of expiration of the tested medicines in the cabinet is reduced.
As shown in fig. 5, in some embodiments, a clinical trial drug management method for a smart drug cabinet further comprises:
s110, receiving a recovery list of the to-be-recovered tested medicines, wherein the recovery list comprises third tested medicine information;
specifically, the drug to be recovered is the rest drug to be recovered, which is already issued and is subjected to clinical test termination or completion, and a unique electronic tag still exists on the drug to be recovered, and the electronic tag contains the identity information of the drug;
s111, when detecting that the to-be-recovered tested medicine is placed on the bearing table, acquiring second weight change information corresponding to the pressure sensor;
the second weight change information may be a specific value, for example, the weight of the drug to be recovered, or a signal, for example, a fluctuation signal for detecting a change in the pressure value.
And S112, when the cabinet door is detected to be closed, the RFID reader-writer scans the electronic tag of the to-be-recovered tested medicine, acquires tag information of the to-be-recovered tested medicine and matches the tag information with the third tested medicine information, and if the matching is successful, acquires the position information of the to-be-recovered tested medicine according to the tag information and the second weight change information of the to-be-recovered tested medicine.
In some embodiments, if the read label information of the drug to be recovered matches the third drug information, it indicates that the drug to be recovered in the cabinet is a drug in the recovery list, and the specific position of the drug to be recovered in the cabinet is determined in combination with the change of the pressure sensor.
Further, before the step of acquiring the second weight change information corresponding to the pressure sensor when it is detected that the test medicine to be recovered is placed on the loading table, it further includes:
and acquiring the position information of the tested medicine to be recovered according to the position information of the tested medicine corresponding to the second tested medicine information, and prompting a bearing table corresponding to the tested medicine to be recovered according to the third tested medicine information and the position information of the tested medicine to be recovered.
In the process of recovering the tested medicine, the tested medicine has one piece of position information when being dispensed, so that the tested medicine to be recovered can be recovered in situ according to the previously bound position information after the clinical test is finished, the tested medicine to be recovered is recovered into the cabinet body more quickly and accurately, the classification is convenient, the order is ensured, and the storage pressure of the storage database is reduced.
As shown in fig. 6, in some embodiments, a clinical trial drug management method for a smart drug cabinet further comprises:
s210, generating a return list of the tested medicines according to the third tested medicine information and/or the expired medicine information;
the information of the to-be-recovered tested medicines and the expired medicines comprise the information of names, validity periods, commodities, codes, specification models, batch numbers, departments and the like of the medicines.
Specifically, the third test drug information is information of the to-be-recovered test drug, and when the to-be-recovered test drug is put into the cabinet corresponding to the third test drug information and recovered, a recovery list is automatically generated, and a worker waits for cleaning and recovering the to-be-recovered drug in the cabinet; the medicine to be recovered in the cabinet can be cleaned in time, and the space is cleaned.
In some embodiments, the cabinet further includes expired tested drugs, the RFID reader can obtain the validity period of the tested drugs after scanning and reading the label information of the tested drugs, and when the preset validity period in the cabinet is compared with the validity period of the tested drugs (for example, the expired drugs in the month before the validity period), the expired drugs can be screened out, the expired drug information is generated and synchronized to the return list, and the staff is waited to clear and return. The medicine expiration date in the cabinet can be monitored, expired medicines are prevented from flowing into clinical experiments, and the medicines can be cleaned in time, so that dynamic update of the medicines in the cabinet is ensured.
S211, when the cabinet door is detected to be opened, prompting a bearing table corresponding to the tested medicine to be recovered according to the third tested medicine information and the position information of the tested medicine to be recovered; and/or prompting the bearing table corresponding to the expired tested medicine according to the expired medicine information and the position information of the tested medicine.
If staff needs to open the cabinet to return the to-be-recovered tested medicine, after clicking the screen recovery list, the cabinet door is opened, the to-be-recovered tested medicine is automatically identified as a position according to the return list, a prompt is given on a corresponding bearing table, the staff can quickly find out and take away the return, the opening time of the cabinet door can be reduced, and the temperature return time of the to-be-recovered tested medicine is reduced.
Likewise, the return steps of the expired test drug are not described in any great detail. The test medicine to be recovered can be recovered together with the expired medicine or separately recovered.
As shown in fig. 7, in some embodiments, a clinical trial drug management method for a smart drug cabinet further comprises:
s310, receiving a return list of the tested medicines;
s311, determining whether the returned medicine in the cabinet is complete according to the returned list of the tested medicine;
s312, after the return medicine returned to the cabinet is determined to be complete, a return prompt is sent.
Furthermore, in some embodiments, the inventive arrangements further comprise the steps of: when the cabinet door is closed, whether the taken returned tested medicine is correct or not is automatically identified, and if not, a warning prompt is sent out.
After the staff takes the corresponding medicines according to the return list, the cabinet door is closed, the RFID reader automatically scans the electronic tags of the residual medicines in the cabinet, reads the tag information and compares the tag information with the tag information of the previous time, finds the reduced tag information, and can obtain the tested medicines corresponding to the return medicine cabinet, so that the correctness of the return can be identified.
In some embodiments, the cabinet body includes an upper cabinet and a lower cabinet, and before the step of acquiring the first weight change information corresponding to the pressure sensor when the test medicine is detected to be placed on the carrying table, the method further includes:
according to the first tested medicine information and the position information of the tested medicine in the current cabinet body, the position information of the same kind of medicine as the tested medicine is obtained, the tested medicine is distributed to the corresponding bearing table, and the cabinet door of the upper cabinet or the lower cabinet is correspondingly opened.
Inquiring the medicine storage position in the medicine cabinet which is the same medicine as the tested medicine, putting the tested medicine in the same layer, and can better concentrate and classify the tested medicine in the cabinet, thereby facilitating the subsequent searching and checking, and also facilitating the subsequent medicine taking only by opening a cabinet door of a certain layer without opening two layers respectively, and reducing the door opening time.
Still further, the method further comprises: if the upper cabinet and the lower cabinet are provided with the tested medicine corresponding to the first tested medicine information, acquiring the current weight information of the loading table which is the same medicine as the tested medicine in the cabinet body, distributing the tested medicine to the loading table with the minimum weight, and opening the cabinet door of the corresponding upper cabinet or lower cabinet.
According to the weight of each layer of plummer in the drug cabinet, put into the one deck of minimum weight with the test drug, be convenient for ensure that the bearing weight of each layer of plummer in the intelligent drug cabinet is controllable and even, avoid too much medicine to pile up at same layer and lead to crowded messenger's temperature in certain layer space to and avoid medicine to pile up and lead to RFID reading's rate of accuracy and speed to reduce.
In some embodiments, before acquiring the first weight change information corresponding to the pressure sensor when the test drug is detected to be placed on the carrier table, the method further comprises:
if the types of the tested medicines corresponding to the first tested medicine information are multiple, the current weight information of the cabinet body and each layer of bearing table is obtained, the multiple tested medicines are distributed to the bearing table with the minimum weight, and the cabinet door of the corresponding upper cabinet or lower cabinet is opened.
When medicines are supplemented into the cabinet, various tested medicines to be supplemented are obtained according to the cabinet-entering list, and then the cabinet-entering operation needs to be completed once in order to reduce the cabinet-opening time, and after the cabinet is opened, a worker simultaneously places the various tested medicines into the medicine cabinet, and places the various medicines into one layer as much as possible; specifically, according to the current weight information of each layer of plummer in the cabinet body, the plummer with the minimum weight is preferentially distributed, the space which can accommodate various medicines can be reserved, the space in the medicine cabinet is ensured to be uniform, after the plummer with the same layer is put in, the corresponding pressure sensor only records the weight change information once, and after the cabinet door is closed, the plummer with the minimum weight can be identified, and the various medicines can be fed into the plummer with the minimum weight, so that the subsequent positioning and searching are facilitated.
In addition, this intelligent medicine cabinet still has medicine and traces back the function to know the whole flow stage of the medicine that receives test, can obtain the current stage that receives test through the mode of the RFID sign indicating number of input medicine binding or scanning electronic tags.
The application also provides a clinical trial medicine management system for the intelligent medicine cabinet, which comprises: the device comprises a list acquisition unit, a weight change information acquisition unit and a tested drug grade position determination unit;
the list acquisition unit is used for receiving a cabinet entering list of the tested medicines and a dispensing list of the tested medicines, wherein the cabinet entering list comprises first tested medicine information, and the tested medicines are provided with unique electronic tags; the release list comprises subject information and second test drug information;
the weight change information acquisition unit is used for acquiring weight change information of the corresponding pressure sensor when detecting that the tested medicine is placed on the bearing table;
the test medicine grade position determining unit is used for scanning the electronic tag of the test medicine when the cabinet door is detected to be closed, acquiring tag information of the test medicine and matching the tag information with the first test medicine information, acquiring position information of the test medicine according to the tag information of the test medicine and the first weight change information if matching is successful, and prompting a bearing table corresponding to the test medicine according to the second test medicine information and the position information of the test medicine when the cabinet door is detected to be opened.
The application also proposes a readable storage medium storing a computer program which, when executed by a processor, causes the processor to perform the steps of:
receiving a cabinet entering list of tested medicines, wherein the cabinet entering list comprises first tested medicine information, and the tested medicines are provided with unique electronic tags;
when detecting that the tested medicine is put on the bearing table, acquiring first weight change information corresponding to the pressure sensor;
when the cabinet door is detected to be closed, the RFID reader-writer scans the electronic tag of the tested medicine, acquires tag information of the tested medicine and matches the tag information with the first tested medicine information;
if the matching is successful, acquiring the position information of the tested medicine according to the label information and the first weight change information of the tested medicine;
receiving a dispensing list of the test drug, the dispensing list including subject information and second test drug information;
when the cabinet door is detected to be opened, the bearing table corresponding to the tested medicine is prompted according to the second tested medicine information and the position information of the tested medicine.
The application also provides an intelligent medicine cabinet, which comprises a cabinet body, wherein the cabinet body comprises a memory and a processor, the memory stores a computer program, and when the computer program is executed by the processor, the processor is caused to execute the following steps:
receiving a cabinet entering list of tested medicines, wherein the cabinet entering list comprises first tested medicine information, and the tested medicines are provided with unique electronic tags;
when detecting that the tested medicine is put on the bearing table, acquiring first weight change information corresponding to the pressure sensor;
when the cabinet door is detected to be closed, the RFID reader-writer scans the electronic tag of the tested medicine, acquires tag information of the tested medicine and matches the tag information with the first tested medicine information;
if the matching is successful, acquiring the position information of the tested medicine according to the label information and the first weight change information of the tested medicine;
receiving a dispensing list of the test drug, the dispensing list including subject information and second test drug information;
when the cabinet door is detected to be opened, the bearing table corresponding to the tested medicine is prompted according to the second tested medicine information and the position information of the tested medicine.
Those skilled in the art will appreciate that implementing all or part of the above-described methods in accordance with the embodiments can be accomplished by way of a computer program stored on a non-transitory computer readable storage medium, which when executed, can comprise the steps of the above-described embodiments of the methods.
Any reference to memory, storage, database, or other medium used in embodiments provided herein may include non-volatile and/or volatile memory. The nonvolatile memory can include Read Only Memory (ROM), programmable ROM (PROM), electrically Programmable ROM (EPROM), electrically Erasable Programmable ROM (EEPROM), or flash memory. Volatile memory can include Random Access Memory (RAM) or external cache memory. By way of illustration and not limitation, RAM is available in a variety of forms such as Static RAM (SRAM), dynamic RAM (DRAM), synchronous DRAM (SDRAM), double Data Rate SDRAM (DDRSDRAM), enhanced SDRAM (ESDRAM), synchronous Link DRAM (SLDRAM), memory bus direct RAM (RDRAM), direct memory bus dynamic RAM (DRDRAM), and memory bus dynamic RAM (RDRAM), among others.
The technical features of the above embodiments can be arbitrarily combined, and all possible combinations of the technical features in the above embodiments are not described for brevity of description, however, as long as there is no contradiction between the combinations of the technical features, they should be considered as the scope of the description.
The foregoing examples illustrate only a few embodiments of the application and are described in detail herein without thereby limiting the scope of the application. It should be noted that it is possible for those skilled in the art to make several variations and modifications without departing from the spirit of the application, and these are all the preferred embodiments of the application, and it is needless to say that the scope of the claims of the application shall not be limited thereto, and therefore equivalent variations according to the claims of the application shall still fall within the scope of the application.
Claims (10)
1. The utility model provides a clinical trial medicine management method for intelligent medicine cabinet, intelligent medicine cabinet includes cabinet body, RFID read write line, a plurality of plummer and a plurality of pressure sensor, the RFID read write line sets up in the cabinet body, a plurality of pressure sensor respectively one by one with a plurality of plummer corresponds, its characterized in that, the method includes:
receiving a cabinet entering list of tested medicines, wherein the cabinet entering list comprises first tested medicine information, and the tested medicines are provided with unique electronic tags;
when the tested medicine is detected to be placed on the bearing table, acquiring first weight change information corresponding to the pressure sensor;
when the cabinet door is detected to be closed, the RFID reader-writer scans the electronic tag of the tested medicine, acquires tag information of the tested medicine and matches the tag information with the first tested medicine information;
if the matching is successful, acquiring the position information of the tested medicine according to the label information of the tested medicine and the first weight change information;
receiving a release list of the tested drugs, wherein the release list comprises subject information and second tested drug information;
when the cabinet door is detected to be opened, the bearing table corresponding to the tested medicine is prompted according to the second tested medicine information and the position information of the tested medicine.
2. The method of clinical trial medication management for an intelligent drug cabinet of claim 1, further comprising:
receiving a recovery list of the to-be-recovered test drug, wherein the recovery list comprises third test drug information;
when the to-be-recovered tested medicine is detected to be placed on the bearing table, second weight change information corresponding to the pressure sensor is obtained;
when the cabinet door is detected to be closed, the RFID reader-writer scans the electronic tag of the to-be-recovered tested medicine, acquires tag information of the to-be-recovered tested medicine and matches the tag information with the third tested medicine information, and if matching is successful, acquires the position information of the to-be-recovered tested medicine according to the tag information of the to-be-recovered tested medicine and the second weight change information.
3. The method for clinical trial drug management of a smart drug cabinet of claim 2, further comprising:
generating a return list of the tested medicines according to the third tested medicine information and/or the expired medicine information;
when the cabinet door is detected to be opened, prompting a bearing table corresponding to the tested medicine to be recovered according to the third tested medicine information and the position information of the tested medicine to be recovered; and/or prompting a bearing table corresponding to the expired tested medicine according to the expired medicine information and the position information of the tested medicine.
4. The method of claim 1, wherein the cabinet body comprises an upper cabinet and a lower cabinet, and wherein before the step of acquiring the first weight change information corresponding to the pressure sensor when the test drug is detected to be placed on the loading stand, the method further comprises:
and according to the first tested medicine information and the position information of the tested medicine in the current cabinet body, acquiring the position information of the same kind of medicine as the tested medicine, distributing the tested medicine to the corresponding bearing table, and correspondingly opening the cabinet door of the upper cabinet or the lower cabinet layer.
5. The method for clinical trial drug management of a smart drug cabinet of claim 4,
according to the first tested medicine information and the position information of the tested medicine in the current cabinet body, the position information of the same kind of medicine as the tested medicine is obtained, the tested medicine is distributed to a corresponding bearing table, and the cabinet door of the upper cabinet or the lower cabinet layer is correspondingly opened, and the method further comprises the steps of:
if the upper cabinet and the lower cabinet are provided with the tested medicine corresponding to the first tested medicine information, acquiring the current weight information of the bearing table, which is the same medicine as the tested medicine, in the cabinet body, distributing the tested medicine to the bearing table with the minimum weight, and opening the corresponding cabinet door of the upper cabinet or the lower cabinet.
6. The method for clinical trial medication management for a smart drug cabinet of claim 4, wherein prior to the step of obtaining the first weight change information corresponding to the pressure sensor when the subject medication is detected to be placed on the carrier, the method further comprises:
if the types of the tested medicines corresponding to the first tested medicine information are multiple, the current weight information of each layer of the loading table in the cabinet body is obtained, the multiple tested medicines are distributed to the loading table with the minimum weight, and the corresponding cabinet door of the upper cabinet or the lower cabinet is opened.
7. The method of claim 1, wherein a delivery list of the subject drugs is received, the delivery list including subject information and second subject drug information, and wherein the method further comprises:
determining a matching list of the subject and the test drug according to the subject information and the second test drug information:
acquiring the corresponding relation between the subject and the tested medicine according to the matching list of the subject and the tested medicine;
determining whether the dispensed test drug is correct according to the corresponding relation between the subject and the test drug; wherein, the corresponding relation is a one-to-one or one-to-many matching relation between the subject and the tested medicine.
8. The method for clinical trial medication management for an intelligent drug cabinet of claim 7, wherein the determining whether the cabinet of the subject medication is correct based on the correspondence between the subject and the subject medication, before the method further comprises:
when the inventory of the tested medicines matched with the subjects is at least two, acquiring one of the tested medicines with the shortest near-term;
and prompting the corresponding bearing table of the tested drug with the shortest near-term according to the second tested drug information and the position information of the tested drug.
9. The method for clinical trial medication management for an intelligent drug cabinet of claim 2, wherein prior to the step of obtaining second weight change information corresponding to the pressure sensor when the test medication to be retrieved is detected to be placed on the carrier, the method further comprises:
and acquiring the position information of the tested medicine to be recovered according to the position information of the tested medicine corresponding to the second tested medicine information, and prompting the bearing table corresponding to the tested medicine to be recovered according to the third tested medicine information and the position information of the tested medicine to be recovered.
10. A clinical trial drug management system for an intelligent drug cabinet, the system comprising: the device comprises a list acquisition unit, a weight change information acquisition unit and a tested drug grade position determination unit;
the list acquisition unit is used for receiving a cabinet entering list of the tested medicines and a dispensing list of the tested medicines, wherein the cabinet entering list comprises first tested medicine information, and the tested medicines are provided with unique electronic tags; the release list comprises subject information and second test drug information;
the weight change information acquisition unit is used for acquiring weight change information of the corresponding pressure sensor when the tested medicine is detected to be placed on the bearing table;
the test medicine grade position determining unit is used for scanning the electronic tag of the test medicine when the cabinet door is detected to be closed, acquiring tag information of the test medicine and matching the tag information with the first test medicine information, acquiring position information of the test medicine according to the tag information of the test medicine and the first weight change information if matching is successful, and prompting a bearing table corresponding to the test medicine according to the second test medicine information and the position information of the test medicine when the cabinet door is detected to be opened.
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|---|---|---|---|
| CN202310851538.2A CN116825310A (en) | 2023-07-12 | 2023-07-12 | Clinical trial medicine management method and system for intelligent medicine cabinet |
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| CN202310851538.2A CN116825310A (en) | 2023-07-12 | 2023-07-12 | Clinical trial medicine management method and system for intelligent medicine cabinet |
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